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Alexandros Papadimitriou

Research Profile

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Greece

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Physiology

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Infants

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Publications

TOP 3
Ioannis Z Kapsalakis; Gregory P Lee; Alexandros Papadimitriou; Joe Sam Robinson; Panagiotis Toulas; Dimitrios Verganelakis; Indug Chung; Ioannis Fezoulidis; Efstathios D Gotsis; Georgios Hadjigeorgiou; Eftychia Z Kapsalaki; Kostas N Fountas
Preoperative evaluation with FMRI of patients with intracranial gliomas.
Alexandros Papadimitriou; Polyxeni Nicolaidou; Andreas Fretzayas; George P Chrousos
Clinical review: Constitutional advancement of growth, a.k.a. early growth acceleration, predicts early puberty and childhood obesity.
Konstantinos Aggelakis; Fani Zacharaki; Efthimios Dardiotis; Georgia Xiromerisiou; Vana Tsimourtou; Styliani Ralli; Maria Gkaraveli; Dimitris Bourpoulas; Paraskevi Rodopoulou; Alexandros Papadimitriou; Georgios M Hadjigeorgiou
Interleukin-1B and interleukin-1 receptor antagonist gene polymorphisms in Greek multiple sclerosis (MS) patients with bout-onset MS.

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All Publications

2012: Ioannis Z Kapsalakis; Gregory P Lee; Alexandros Papadimitriou; Joe Sam Robinson; Panagiotis Toulas; Dimitrios Verganelakis; Indug Chung; Ioannis Fezoulidis; Efstathios D Gotsis; Georgios Hadjigeorgiou; Eftychia Z Kapsalaki; Kostas N Fountas
Preoperative evaluation with FMRI of patients with intracranial gliomas.
Radiology research and practice 2012;2012():727810.
2010: Alexandros Papadimitriou; Polyxeni Nicolaidou; Andreas Fretzayas; George P Chrousos
Clinical review: Constitutional advancement of growth, a.k.a. early growth acceleration, predicts early puberty and childhood obesity.
The Journal of clinical endocrinology and metabolism 2010;95(10):4535-41.
2010: Konstantinos Aggelakis; Fani Zacharaki; Efthimios Dardiotis; Georgia Xiromerisiou; Vana Tsimourtou; Styliani Ralli; Maria Gkaraveli; Dimitris Bourpoulas; Paraskevi Rodopoulou; Alexandros Papadimitriou; Georgios M Hadjigeorgiou
Interleukin-1B and interleukin-1 receptor antagonist gene polymorphisms in Greek multiple sclerosis (MS) patients with bout-onset MS.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2010;31(3):253-7.
2009: Alexandros Papadimitriou; M Konstantinidou; H Christopanou; Paraskevi Xepapadaki; O Giannouli; Polyxeni Nicolaidou
Secular trend in body height of schoolchildren in Northeast Attica, Greece.
Journal of pediatric endocrinology & metabolism : JPEM 2009;22(1):13-7.
2008: Alexandros Papadimitriou; Soula Pantsiotou; Konstantinos Douros; Dimitrios T Papadimitriou; Polyxeni Nicolaidou; Andreas Fretzayas
Timing of pubertal onset in girls: evidence for non-Gaussian distribution.
The Journal of clinical endocrinology and metabolism 2008;93(11):4422-5.
2008: Roberta Virgilio; Dario Ronchi; Georgios M Hadjigeorgiou; Alessandra Bordoni; Francesca Saladino; Maurizio Moggio; Laura Adobbati; Demetra Kafetsouli; Evangelia Tsironi; Stefano C Previtali; Alexandros Papadimitriou; Nereo Bresolin; Giacomo P Comi
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia.
Journal of neurology 2008;255(9):1384-91.
2008: Alexandros Papadimitriou; Grigorios Fytanidis; Konstantinos Douros; Dimitrios T Papadimitriou; Polyxeni Nicolaidou; Andreas Fretzayas
Greek young men grow taller.
Acta paediatrica (Oslo, Norway : 1992) 2008;97(8):1105-7.
2008: Alexandros Papadimitriou; Grigorios Fytanidis; Konstantinos Douros; Chryssa Bakoula; Polyxeni Nicolaidou; Andreas Fretzayas
Age at menarche in contemporary Greek girls: evidence for levelling-off of the secular trend.
Acta paediatrica (Oslo, Norway : 1992) 2008;97(6):812-5.
2008: Georgia Xiromerisiou; Georgios M Hadjigeorgiou; Alexandros Papadimitriou; Evaggelos Katsarogiannis; Vasiliki Gourbali; Andrew Singleton
Association between AKT1 gene and Parkinson's disease: a protective haplotype.
Neuroscience letters 2008;436(2):232-4.
2008: S Pantsiotou; Alexandros Papadimitriou; Konstantinos Douros; Kostas Priftis; Polyxeni Nicolaidou; Andreas Fretzayas
Maturational tempo differences in relation to the timing of the onset of puberty in girls.
Acta paediatrica (Oslo, Norway : 1992) 2008;97(2):217-20.
2008: Efthimios Dardiotis; Georgios M Hadjigeorgiou; Maria Dardioti; Nikolaos Scarmeas; K Paterakis; Konstantinos Aggelakis; A Komnos; A Tasiou; Georgia Xiromerisiou; I Gabranis; E Zintzaras; Alexandros Papadimitriou; Apostolos H Karantanas
Alpha-1 antichymotrypsin gene signal peptide a/t polymorphism and primary intracerebral hemorrhage.
European neurology 2008;59(6):307-14.
2008: Alexandros Papadimitriou; Alexandra Mihaela Dumitrescu; Antigone Papavasiliou; Andreas Fretzayas; Polyxeni Nicolaidou; Samuel Refetoff
A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay.
Pediatrics 2008;121(1):e199-202.
2007: Alexandros Papadimitriou; Dimitrios T Papadimitriou; Anna Papadopoulou; Polyxeni Nicolaidou; Andreas Fretzayas
Low TSH levels are not associated with osteoporosis in childhood.
European journal of endocrinology / European Federation of Endocrine Societies 2007;157(2):221-3.
2007: Nikolaos Dimopoulos; Christina Piperi; Aristea Salonicioti; Vassiliki Psarra; Flerri Gazi; Alexandros Papadimitriou; Robert W Lea; Anastasios Kalofoutis
Correlation of folate, vitamin B12 and homocysteine plasma levels with depression in an elderly Greek population.
Clinical biochemistry 2007;40(9-10):604-8.
2007: Katerina Papachroni; Natalia Ninkina; Aggeliki Papapanagiotou; Georgios M Hadjigeorgiou; Georgia Xiromerisiou; Alexandros Papadimitriou; Anastasios Kalofoutis; Vladimir L Buchman
Autoantibodies to alpha-synuclein in inherited Parkinson's disease.
Journal of neurochemistry 2007;101(3):749-56.
2007: Polyxeni Nicolaidou; Artemis Tsitsika; Alexandros Papadimitriou; A Karantana; Anna Papadopoulou; Fotini Psychou; D Liakopoulou; Helen Georgouli; Talia Kakourou; George Chrousos
Hereditary vitamin D-resistant rickets in Greek children: genotype, phenotype, and long-term response to treatment.
Journal of pediatric endocrinology & metabolism : JPEM 2007;20(3):425-30.
2007: Georgia Xiromerisiou; Georgios M Hadjigeorgiou; Vanessa Gourbali; J Johnson; I Papakonstantinou; Alexandros Papadimitriou; Andrew Singleton
Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2007;14(1):7-11.
2007: Alexandros Papadimitriou; Konstantinos Douros; Andreas Fretzayas; Polyxeni Nicolaidou
The secular trend of body weight of Greek schoolchildren in the 20th century.
Medical science monitor : international medical journal of experimental and clinical research 2007;13(1):RA8-11.
2007: Polyxeni Nicolaidou; Anna Papadopoulou; Yiannis G Matsinos; Helen Georgouli; Andreas Fretzayas; Alexandros Papadimitriou; Kostas Priftis; Konstantinos Douros; George Chrousos
Vitamin D receptor polymorphisms in hypocalcemic vitamin D-resistant rickets carriers.
Hormone research 2007;67(4):179-83.
2006: Alexandros Papadimitriou; Theodora Gousi; Olga Giannouli; Polyxeni Nicolaidou
The growth of children in relation to the timing of obesity development.
Obesity (Silver Spring, Md.) 2006;14(12):2173-6.
2006: Alexandros Papadimitriou; Dionysia Kounadi; Maria Konstantinidou; Paraskevi Xepapadaki; Polyxeni Nicolaidou
Prevalence of obesity in elementary schoolchildren living in Northeast Attica, Greece.
Obesity (Silver Spring, Md.) 2006;14(7):1113-7.
2006: Alexandros Papadimitriou; Despina Beri; Alexandra Tsialla; Andreas Fretzayas; Fotini Psychou; Polyxeni Nicolaidou
Early growth acceleration in girls with idiopathic precocious puberty.
The Journal of pediatrics 2006;149(1):43-6.
2006: Elli Anagnostou; Dimitrios Mandellos; G Limbitaki; Alexandros Papadimitriou; Dimitri Anastasopoulos
Positional nystagmus and vertigo due to a solitary brachium conjunctivum plaque.
Journal of neurology, neurosurgery, and psychiatry 2006;77(6):790-2.
2006: Alexandros Papadimitriou; Despina Beri; Polyxeni Nicolaidou
Isolated scrotal hair in infancy.
The Journal of pediatrics 2006;148(5):690-1.
2006: Georgios M Hadjigeorgiou; Georgia Xiromerisiou; Vanessa Gourbali; Konstantinos Aggelakis; Nikolaos Scarmeas; Alexandros Papadimitriou; Andrew Singleton
Association of alpha-synuclein Rep1 polymorphism and Parkinson's disease: influence of Rep1 on age at onset.
Movement disorders : official journal of the Movement Disorder Society 2006;21(4):534-9.
2006: Sonja Scholz; Georgia Xiromerisiou; Hon-Chung Fung; Johanna Eerola; Olli Hellström; Alexandros Papadimitriou; Georgios M Hadjigeorgiou; Pentti J Tienari; Hubert H Fernandez; Ronald Mandel; Michael S Okun; Katrina Gwinn-Hardy; Andrew Singleton
The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations.
Neuroscience letters 2006;395(3):227-9.
2006: Sara Galbiati; Andreina Bordoni; Dimitra Papadimitriou; Antonio Toscano; Carmelo Rodolico; Efi Katsarou; Monica Sciacco; Anastasia Garufi; Alessandro Prelle; M 'hammed Aguennouz; Maria Bonsignore; Crimi Marco; Andrea Martinuzzi; Nereo Bresolin; Alexandros Papadimitriou; Giacomo P Comi
New mutations in TK2 gene associated with mitochondrial DNA depletion.
Pediatric neurology 2006;34(3):177-85.
2006: Hon-Chung Fung; Georgia Xiromerisiou; J Raphael Gibbs; Y R Wu; Johanna Eerola; Vanessa Gourbali; Olli Hellström; C M Chen; Jaime Duckworth; Alexandros Papadimitriou; Pentti J Tienari; Georgios M Hadjigeorgiou; John Hardy; Andrew Singleton
Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts.
Neuro-degenerative diseases 2006;3(6):327-33.
2006: Daniela Perani; Valentina Garibotto; Georgios M Hadjigeorgiou; Dimitra Papadimitriou; Ferruccio Fazio; Alexandros Papadimitriou
Positron emission tomography changes in PARK1 mutation.
Movement disorders : official journal of the Movement Disorder Society 2006;21(1):127-30.
2005: Alexandros Papadimitriou; George Chrousos
Reconsidering the sex differences in the incidence of pubertal disorders.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2005;37(11):708-10.
2005: Georgios M Hadjigeorgiou; Konstantinos N Paterakis; Efthimios Dardiotis; Maria Dardioti; Konstantinos Aggelakis; A Tasiou; Georgia Xiromerisiou; A Komnos; E Zintzaras; Nikolaos Scarmeas; Alexandros Papadimitriou; Apostolos H Karantanas
IL-1RN and IL-1B gene polymorphisms and cerebral hemorrhagic events after traumatic brain injury.
Neurology 2005;65(7):1077-82.
2005: Dimitrios Mandellos; G Limbitaki; Alexandros Papadimitriou; Dimitri Anastasopoulos
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a Greek family.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2005;26(4):278-81.
2005: Jordi Clarimon; Georgia Xiromerisiou; Johanna Eerola; Vanessa Gourbali; Olli Hellström; Euthimios Dardiotis; Terhi Peuralinna; Alexandros Papadimitriou; Georgios M Hadjigeorgiou; Pentti J Tienari; Andrew Singleton
Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.
BMC neurology 2005;5():11.
2004: Amalia Sertedaki; Alexandros Papadimitriou; Antonis Voutetakis; A Dracopoulou; Maria Maniati-Christidi; Catherine Dacou-Voutetakis
Gene symbol: TSH B. Disease: congenital hypothyroidism.
Human genetics 2004;115(2):174.
2004: D G Podikoglou; TG Avramidis; Alexandros Papadimitriou
Blink reflex in primary lateral sclerosis.
Journal of neurology, neurosurgery, and psychiatry 2004;75(7):1064-5.
2004: Georgios M Hadjigeorgiou; Apostolos H Karantanas; Aristidis H Zibis; Efthimios Dardiotis; Konstantinos Aggelakis; Alexandros Papadimitriou; Konstantinos N Malizos
Increased frequency of white matter lesions in patients with osteonecrosis (WMLeOn) of the femoral head.
European journal of radiology 2004;50(3):278-84.
2004: Crimi Marco; Alexandros Papadimitriou; Sara Galbiati; Phani Palamidou; Francesco Fortunato; Andreina Bordoni; Urania Papandreou; Dimitra Papadimitriou; Georgios M Hadjigeorgiou; Eurydiki Drogari; Nereo Bresolin; Giacomo P Comi
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethality.
Pediatric research 2004;55(5):842-6.
2003: Emmanuel Kanavakis; Athina Xaidara; Dimitra Papathanasiou-Klontza; Alexandros Papadimitriou; Stavroula Velentza; Sotiris Youroukos
Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait.
Developmental medicine and child neurology 2003;45(12):833-6.
2002: Amalia Sertedaki; Alexandros Papadimitriou; Antonis Voutetakis; Maria Dracopoulou; Maria Maniati-Christidi; Catherine Dacou-Voutetakis
Low TSH congenital hypothyroidism: identification of a novel mutation of the TSH beta-subunit gene in one sporadic case (C85R) and of mutation Q49stop in two siblings with congenital hypothyroidism.
Pediatric research 2002;52(6):935-41.
2002: Georgios M Hadjigeorgiou; Menachem Sadeh; Olimpia Musumeci; Ron Dabby; Laura De Girolami; Ali Naini; Alexandros Papadimitriou; Sara Shanske; Salvatore DiMauro
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families.
Neuromuscular disorders : NMD 2002;12(9):824-7.
2002: Georgios M Hadjigeorgiou; Alexandros Papadimitriou; Olimpia Musumeci; Konstantinos N Paterakis; Konstantina Flabouriari; Sara Shanske; Salvatore DiMauro
A new stop codon mutation (Y52X) in the myophosphorylase gene in a Greek patient with McArdle's disease.
Journal of the neurological sciences 2002;194(1):83-6.
2002: Alexandros Papadimitriou; N Stephanou; K Papantzimas; G Glynos; P Philippidis
Sexual maturation of Greek boys.
Annals of human biology 2002;29(1):105-8.
2001: Laura Napoli; Andreina Bordoni; M Zeviani; Georgios M Hadjigeorgiou; Monica Sciacco; Valeria Tiranti; AE Terentiou; Maurizio Moggio; Alexandros Papadimitriou; Guglielmo Scarlato; Giacomo P Comi
A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family.
Neurology 2001;57(12):2295-8.
2001: Alexandros Papadimitriou
Sex differences in the secular changes in pubertal maturation.
Pediatrics 2001;108(4):E65.
2001: Monica Sciacco; Alessandro Prelle; Giacomo P Comi; Laura Napoli; Alessandro Battistel; Nereo Bresolin; Lucia Tancredi; Costanza Lamperti; Andreina Bordoni; Gigliola Fagiolari; Patrizia Ciscato; Luca Chiveri; Maria Paola Perini; Francesco Fortunato; L Adobbati; S Messina; Antonio Toscano; Filippo Martinelli Boneschi; Alexandros Papadimitriou; Guglielmo Scarlato; Maurizio Moggio
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.
Journal of neurology 2001;248(9):778-88.
2001: Alexandros Papadimitriou; M A Preece; M F Rolland-Cachera; R Stanhope
The anabolic steroid oxandrolone increases muscle mass in prepubertal boys with constitutional delay of growth.
Journal of pediatric endocrinology & metabolism : JPEM 2001;14(6):725-7.
2001: B Aliberti; A Patrikiou; AE Terentiou; S Frangatou; Alexandros Papadimitriou
Spinal cord compression due to extramedullary haematopoiesis in two patients with thalassaemia: complete regression with blood transfusion therapy.
Journal of neurology 2001;248(1):18-22.
2000: E Chroni; Alexandros Papadimitriou; TG Avramidis; AE Terentiou; C Tzioras; R Divari
Stiff-person like syndrome in a patient with multiple pituitary hormone deficiencies.
Acta neurologica Scandinavica 2000;102(6):403-5.
2000: Polyxeni Nicolaidou; G Nyktari; Helen Georgouli; K Athanassaki; Anastasia Garoufi; Alexandros Papadimitriou; Emmanuel Kavazarakis; Themistocles Karpathios
Atrial natriuretic peptide in children with idiopathic hypercalciuria.
Pediatric nephrology (Berlin, Germany) 2000;14(8-9):853-5.
1999: Georgios M Hadjigeorgiou; Giacomo P Comi; Andreina Bordoni; J Shen; Y T Chen; Sabrina Salani; Antonio Toscano; Francesco Fortunato; Sabrina Lucchiari; Nereo Bresolin; Carmelo Rodolico; M G Piscaglia; L Franceschina; Alexandros Papadimitriou; Guglielmo Scarlato
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa.
Journal of inherited metabolic disease 1999;22(6):762-3.
1999: Alexandros Papadimitriou; E Gousia; E Pitaouli; G Tapaki; P Philippidis
Age at menarche in Greek girls.
Annals of human biology 1999;26(2):175-7.
1999: Alexandros Papadimitriou; V Veletza; Georgios M Hadjigeorgiou; A Patrikiou; M Hirano; IE Anastasopoulos
Mutated alpha-synuclein gene in two Greek kindreds with familial PD: incomplete penetrance?
Neurology 1999;52(3):651-4.
1998: Alexandros Papadimitriou; E Chroni; IE Anastasopoulos; TG Avramidis; Georgios M Hadjigeorgiou; M Koutroumanidis
Continuous muscle fiber activity associated with morphea (localized scleroderma).
Neurology 1998;51(6):1763-4.
1998: TG Avramidis; D G Podikoglou; IE Anastasopoulos; M A Koutroumanidis; Alexandros Papadimitriou
Blink reflex in migraine and tension-type headache.
Headache 1998;38(9):691-6.
1998: Alexandros Papadimitriou; Giacomo P Comi; Georgios M Hadjigeorgiou; Andreina Bordoni; Monica Sciacco; Laura Napoli; Alessandro Prelle; Maurizio Moggio; Gigliola Fagiolari; Nereo Bresolin; Sabrina Salani; IE Anastasopoulos; G Giassakis; R Divari; Guglielmo Scarlato
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.
Neurology 1998;51(4):1086-92.
1997: Alexandros Papadimitriou; K Kipourou; C Manta; G Tapaki; P Philippidis
Adipsic hypernatremia syndrome in infancy.
Journal of pediatric endocrinology & metabolism : JPEM 1997;10(5):547-50.
1996: Michael Koutroumanidis; Alexandros Papadimitriou; Evrydiki A Bouzas; T Avramidis; P Papathanassopoulos; R S Howard; T Papapetropoulos
Reduced brain stem excitability in mitochondrial myopathy: evidence for early detection with blink reflex habituation studies.
Muscle & nerve 1996;19(12):1586-95.
1996: Alexandros Papadimitriou; Georgios M Hadjigeorgiou; R Divari; N Papagalanis; G Comi; Nereo Bresolin
The influence of Coenzyme Q10 on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism.
Neuromuscular disorders : NMD 1996;6(1):49-53.
1996: Alexandros Papadimitriou; Georgios M Hadjigeorgiou; P Tsairis; E Papadimitriou; C Ouzounelli; T Ouzounellis
Myoglobinuria due to quail poisoning.
European neurology 1996;36(3):142-5.
1995: Helen Michelakakis; Alexandros Papadimitriou; R Divaris; I Mavridou; Evagelia Dimitriou
Plasma lysosomal enzyme levels in patients with motor neuron disease.
Journal of inherited metabolic disease 1995;18(1):72-4.
1994: N Checcarelli; Alessandro Prelle; Maurizio Moggio; G Comi; Nereo Bresolin; Alexandros Papadimitriou; G Fagiolari; Andreina Bordoni; Guglielmo Scarlato
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy.
Journal of the neurological sciences 1994;123(1-2):74-9.
1993: Evrydiki A Bouzas; D Krasnewich; Michael Koutroumanidis; Alexandros Papadimitriou; J C Marini; Muriel I Kaiser-Kupfer
Ophthalmologic examination in the diagnosis of Proteus syndrome.
Ophthalmology 1993;100(3):334-8.
1993: Priscille Divry; C Jakobs; Christine Vianey-Saban; K M Gibson; Helen Michelakakis; Alexandros Papadimitriou; R Divari; Brigitte Chabrol; M A Cournelle; Marie-Odile Livet
L-2-hydroxyglutaric aciduria: two further cases.
Journal of inherited metabolic disease 1993;16(3):505-7.
1991: Alexandros Papadimitriou; S Servidei
Late onset lipid storage myopathy due to multiple acyl CoA dehydrogenase deficiency triggered by valproate.
Neuromuscular disorders : NMD 1991;1(4):247-52.
1990: Alexandros Papadimitriou; P Manta; R Divari; A Karabetsos; E Papadimitriou; Nereo Bresolin
McArdle's disease: two clinical expressions in the same pedigree.
Journal of neurology 1990;237(4):267-70.